The association between SLC38A3 (Solute Carrier Family 38 Member 3) and Developmental And Epileptic Encephalopathy 102 is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources3
Clinical variants7
Symptoms51
Compounds0
Trials0
Publications2
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.